Home/Recalls/CANADA-51623
Health CanadaType II

LIFEPAK 1000 Defibrillator (2014-06-05)

Published: July 15, 2014Recall ID: 51623Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

LIFEPAK 1000 Defibrillator (2014-06-05)

Additional Source Details

FieldValue
N I D51623
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lifepak-1000-defibrillator-2014-06-05
IssueMedical devices
Title LIFEPAK 1000 Defibrillator (2014-06-05)
Archived1
CategoryMedical devices
Last updated2014-07-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert